A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733707



Internal ID20509637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52811317..52811399hg38UCSC Ensembl
chr4:53677484..53677566hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294947
Samples
Known GenesLOC152578
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733707
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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